College of Forensic Medicine, Health Science Center, Xi'an Jiaotong University, Xi'an, People's Republic of China.
School of Life Science, Northwest A&F University, Yangling, People's Republic of China.
Int J Legal Med. 2021 May;135(3):709-718. doi: 10.1007/s00414-020-02403-z. Epub 2020 Aug 26.
The MiSeq® FGX Forensic system and the HID-Ion AmpliSeq Panel were previously developed for massively parallel sequencing (MPS) for forensic casework. Among the three major sequencing platforms, BGISEQ-500, which is based on multiple PCRs, is still lacking in forensics. Here, a novel forensic panel was constructed to detect 186 single-nucleotide polymorphisms (SNPs) and 123 short tandem repeats (STRs) with MPS technology on the BGISEQ-500™ platform. First, the library preparation, sequencing process, and data analysis were performed, focusing on the average depth of coverage and heterozygote balance. We calculated the allelic frequencies and forensic parameters of STR and SNP loci in 73 unrelated Chinese Han individuals. In addition, performance was evaluated with accuracy, uniformity, sensitivity, PCR inhibitor, repeatability and reproducibility, mixtures, degraded samples, case-type samples, and pedigree analyses. The results showed that 100% accurate and concordant genotypes can be obtained, and the loci with an abundance in the interquartile range accounted for 92.90% of the total, suggesting reliable uniformity in this panel. We obtained a locus detection rate that was higher than 98.78% from 78 pg of input DNA, and the optimal amount was 1.25-10 ng. The maximum concentrations of hematin and humic acid were 200 and 100 μM, respectively (the ratios of detected loci were 96.52% and 92.41%), in this panel. As a mixture, compared with those of SNPs, minor-contributor alleles of STRs could be detected at higher levels. For the degraded sample, the ratio of detected loci was 98.41%, and most profiles from case-type samples were not significantly different in abundance in our studies. As a whole, this panel showed high-performance, reliable, robust, repeatable, and reproducible results, which are sufficient for paternity testing, individual identification, and use for potentially degraded samples in forensic science.
MiSeq® FGX 法医系统和 HID-Ion AmpliSeq 面板最初是为法医工作中的大规模平行测序 (MPS) 而开发的。在这三个主要测序平台中,基于多次 PCR 的 BGISEQ-500 在法医学中仍然缺乏。在这里,我们构建了一个新的法医面板,利用 MPS 技术在 BGISEQ-500™平台上检测 186 个单核苷酸多态性 (SNP) 和 123 个短串联重复 (STR)。首先,我们进行了文库制备、测序过程和数据分析,重点关注平均覆盖深度和杂合子平衡。我们计算了 73 名无关中国汉族个体中 STR 和 SNP 位点的等位基因频率和法医参数。此外,我们还通过准确性、均一性、灵敏度、PCR 抑制剂、重复性和重现性、混合物、降解样本、案例样本和系谱分析来评估性能。结果表明,可获得 100%准确和一致的基因型,并且丰度处于四分位区间内的位点占总位点的 92.90%,表明该面板具有可靠的均一性。我们从 78pg 的输入 DNA 中获得了高于 98.78%的位点检测率,最佳量为 1.25-10ng。该面板中血红素和腐殖酸的最大浓度分别为 200 和 100μM(检测到的位点比例分别为 96.52%和 92.41%)。作为混合物,与 SNP 相比,STR 的次要供体等位基因的检测水平可以更高。对于降解样本,检测到的位点比例为 98.41%,并且在我们的研究中,大多数案例样本的图谱在丰度上没有明显差异。总体而言,该面板表现出高性能、可靠、稳健、可重复和重现性的结果,足以用于亲子鉴定、个体识别以及用于法医学中潜在降解样本。